97754-31-9

Basic information

• Product Name: N-(4-methoxyphenyl)-3-phenylpropanamide
• Synonyms: N-(4-methoxyphenyl)-3-phenylpropanamide
• CAS NO: 97754-31-9
• Molecular Formula: C₁₆H₁₇NO₂
• Molecular Weight: 255.32
• Mol File: 97754-31-9.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-methoxyphenyl)-3-phenylpropanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxyphenyl)-3-phenylpropanamide(97754-31-9)
• EPA Substance Registry System: N-(4-methoxyphenyl)-3-phenylpropanamide(97754-31-9)

Safety Data

• Hazardous Substances Data: 97754-31-9(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 645-45-4 hydrocinnamic acid chloride 
• 51-66-1 4-methoxyacetanilide 
• 100-51-6 benzyl alcohol 
• 501-52-0 3-Phenylpropionic acid 
• 90-04-0 2-methoxy-phenylamine 
• 104-54-1 3-Phenylpropenol 
• 100-42-5 styrene 
• 201230-82-2 carbon monoxide 
• 76228-15-4 N-(4-methoxyphenyl)-3-phenylacrylamide 
• 621-82-9 Cinnamic acid 

Downstream Products

• 71193-46-9 N-(4-methoxyphenyl)-3-phenylpropylamine 
• 918518-74-8 C₁₇H₁₄ClNO 
• 3538-68-9 3-phenylpropanehydrazide 
• 104-94-9 4-methoxy-aniline 
• 27501-84-4 1-(4-methoxyphenyl)-3,4-dihydroquinolin-2(1H)-one 
• 19340-68-2 1-(4-methoxy-phenyl)-4-phenyl-azetidin-2-one 
• 5661-55-2 4-phenylazetidin-2-one 

Relevant articles and documents

Chemoselective reduction of α,β-unsaturated carbonyl compounds in the presence of CuPd alloy nanoparticles decorated on mesoporous graphitic carbon nitride as highly efficient catalyst

Herein, we reported reductions of acid, amide, ester and ketone groups with selectivity (>99%) by the catalytic transfer hydrogenation of with CuPd alloy nanoparticles (NPs) decorated on mesoporous graphitic carbon nitride (Cu50Pd50/mpg-C3N4) catalyst under mild conditions in a water/methanol mixture. CuPd alloy NPs were synthesized by the co-reduction of palladium (II) acetylacetonate and copper(II) acetylacetonate in oleylamine (OAm) solution by the reduction of morpholine-borane solution and then assembled on mpg-C3N4 via liquid phase self‐assembly method. The α, β-unsaturated carbonyl compounds were obtained from the condensation reaction of the benzaldehyde derivatives with acetone derivatives. Cu50Pd50/mpg-C3N4 nanocatalyst was characterized by TEM, XRD, XPS, BET and ICP‐MS. Cu50Pd50/mpg-C3N4 nanocatalyst is highly active catalyst for the reduction of various organic groups and converted to high yield and 99% selectivity. The superior Cu50Pd50/mpg-C3N4 nanocatalyst is highly efficient and reusable catalyst which is reuse after 5 cycle with 98% conversion.

Method for selective reduction α, β - unsaturated carbonyl compound carbon-carbon double bond (by machine translation)

The invention discloses a method for selectively reducing carbon-carbon double bonds in α and β - unsaturated carbonyl compounds, which comprises the following steps of adding α, β - unsaturated carbonyl compounds shown in formula (I) in an electrolysis system and reducing α and β - unsaturated carbonyl compounds with carbonyl-conjugated carbon-carbon double bonds through an electrochemical cathodic reduction reaction. Compared with the reported method, the method disclosed by the invention does not use a metal catalyst and an external oxidant; and the reaction raw material and the electrolyte are low in price, nontoxic and tasteless, simple and convenient in post-treatment. (by machine translation)

Nickel-catalyzed: C-alkylation of thioamide, amides and esters by primary alcohols through a hydrogen autotransfer strategy

A simple catalyst of Ni(OAc)2 and P(t-Bu)3 enables selective C-alkylation of thioacetamides and primary acetamides with alcohols for the first time. Monoalkylation of thioamides, amides and t-butyl esters occurs in excellent yields (>95%). Mechanistic studies reveal that the reaction proceeds via a hydrogen autotransfer pathway. This journal is